Micallef J V, Hayes M M, Latif A, Ahsan R, Sufi S B
World Health Organization Collaborating Centre for Research in Immunoassay, Hammersmith Hospital, London, UK.
Ann Clin Biochem. 1995 Nov;32 ( Pt 6):566-74. doi: 10.1177/000456329503200609.
We studied the serum protein binding of 3H-labelled progesterone, oestradiol and testosterone, and five 125I-labelled analogues of these steroids. All tracers investigated appeared to be bound by proteins in every serum sample tested. The addition of blocking agents caused a substantial reduction in serum protein binding of 3H-labelled steroids, but had relatively little effect on the binding of analogue steroid tracers. Use of analogue steroid tracers in conventional direct immunoassays for oestradiol and progesterone produced anomalous results for some patient samples when compared to extraction radioimmunoassays, but assays where tracer binding to serum constituents was prevented by adoption of two-step procedures appeared to avoid anomalous results. The results suggest that serum protein binding of steroid analogue tracers may be a source of interference in some direct steroid immunoassays.
我们研究了3H标记的孕酮、雌二醇和睾酮以及这几种甾体的五种125I标记类似物的血清蛋白结合情况。在所检测的每个血清样本中,所有研究的示踪剂似乎都与蛋白质结合。加入封闭剂后,3H标记甾体的血清蛋白结合显著减少,但对类似物甾体示踪剂的结合影响相对较小。与萃取放射免疫分析相比,在传统的雌二醇和孕酮直接免疫分析中使用类似物甾体示踪剂时,一些患者样本产生了异常结果,但通过采用两步法防止示踪剂与血清成分结合的分析似乎避免了异常结果。结果表明,甾体类似物示踪剂的血清蛋白结合可能是某些直接甾体免疫分析中干扰的来源。